Medical writing

Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission

Effective Technical Writing & Editing

11 Feb 2020

Also on: 25 Sep 2020

Book by 20 Dec to save
£100 / €140 / $156

This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.

We can customise this course to meet your requirements.

Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive practical medical writing course will benefit participants by enabling them to achieve this standard.

Successful Medical Writing

14-16 Oct 2019

Also on: 18 May 2020

Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, Detailed and Critical Summaries and regulatory submissions

Veterinary Pharmaceutical Submissions in the EU

26-27 Nov 2019

Also on: 24 Mar 2020

This practical four day course provides a comprehensive understanding of a veterinary medicine development in the EU and USA.